Colon Cancer: Gene >> KRIT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000340022
Start	92241109:92241109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.146G>A
AA Mutation	p.Arg49Lys(p.R49K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000340022
Start	92221969:92221969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1496C>T
AA Mutation	p.Pro499Leu(p.P499L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000340022
Start	92235521:92235521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.611A>C
AA Mutation	p.Asn204Thr(p.N204T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000340022
Start	92242059:92242059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs34358665
CDS Mutation	c.77G>A
AA Mutation	p.Arg26Gln(p.R26Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000340022
Start	92237732:92237732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.290T>G
AA Mutation	p.Phe97Cys(p.F97C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000340022
Start	92226548:92226548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1124T>C
AA Mutation	p.Leu375Pro(p.L375P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000340022
Start	92234818:92234818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.835A>G
AA Mutation	p.Thr279Ala(p.T279A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340022
Start	92234553:92234553(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761571988
CDS Mutation	c.885C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340022
Start	92241087:92241087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145901266
CDS Mutation	c.168G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340022
Start	92222007:92222007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1458C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000340022
Start	92235597:92235597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777198867
CDS Mutation	c.535C>T
AA Mutation	p.Arg179Ter(p.R179*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000340022
Start	92236480:92236480(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.418C>T
AA Mutation	p.Arg140Ter(p.R140*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000340022
Start	92241111:92241112(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.143dupA
AA Mutation	p.Arg49GlufsTer15(p.R49Efs*15)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> KRIT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000340022
Start	92226630:92226630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1042C>T
AA Mutation	p.Pro348Ser(p.P348S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340022
Start	92213327:92213327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1893A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000340022
Start	92222005:92222005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1460G>A
AA Mutation	p.Trp487Ter(p.W487*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000340022
Start	92234897:92234897(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.756C>A
AA Mutation	p.Tyr252Ter(p.Y252*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript